Biomimetic adhesive compositions comprising a phenolic polymer and methods for use thereof

ABSTRACT

Biomimetic adhesive compositions can be used in various aspects of subterranean treatment operations. Methods for treating a subterranean formation can comprise: providing an adhesive composition that comprises a first polymer comprising a plurality of monomers that comprise a phenolic moiety, a biopolymer that is crosslinkable with the first polymer, a crosslinking agent, and an oxidizing agent; introducing the adhesive composition into a subterranean formation; and forming a coacervate-bound surface in the subterranean formation by crosslinking the first polymer.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a divisional of U.S. patent application Ser.No. 13/478,910, filed on May 23, 2012.

BACKGROUND

The present disclosure relates to adhesive compositions, and, morespecifically, to biomimetic adhesive compositions and their use in asubterranean formation.

Biological organisms are well known for their ability to construct awide breadth of biomaterials, many of which have properties that areunrivaled by their synthetic counterparts. As used herein, the term“biomaterial” refers to a substance that is synthesized by a biologicalorganism. Biomaterials can be used for a wide variety of purposes bybiological organisms including, for example, support and protection(e.g., endoskeletons, exoskeletons, shells, and like biomineralizedstructures), trapping of prey (e.g., spider webs), locomotion, andsurface adhesion. Self-assembly may play a role in the formation of manyof these biomaterials. As used herein, the term “self-assembly” refersto the spontaneous organization of substances to form stable,well-organized, structurally defined arrays without the influence ofexternal forces.

Study of the structure of biomaterials can provide the inspiration fordesigned synthetic materials. In some cases, a synthetic material canattempt to replicate the structure of a biomaterial. In other cases, asynthetic material can have a significantly different structure than theparent biomaterial, but still incorporate a structural elementtherefrom, sometimes in modified form. Structurally modified syntheticmaterials that retain a structural element or modified structuralelement of a parent biomaterial are often referred to as “biomimeticmaterials.” Modification of the parent biomaterial structure, as inbiomimetic materials, may be beneficial when the parent biomaterial isunsuitable for an intended application due to undesirable propertiessuch as, for example, cost, stability, mechanical properties, physicalproperties, chemical properties, and the like.

Adhesive compositions, in particular, are ubiquitous among biologicalorganisms due to their ability to effectively function in a variety ofenvironments. Marine mussels and other marine organisms, in particular,are known for their ability to secrete adhesive proteins (bioadhesives)that can form a coacervate in the mussels' aqueous habitat. As usedherein, the term “coacervate” refers to an agglomeration of crosslinkedmolecules that adjoins two or more surfaces. Most typically, theseadhesive proteins comprise a DOPA (3,4-dihydroxyphenylalanine) or likecatechol-type moiety within the polymer structure. Without being boundby any theory or mechanism, it is believed that catechol-type moietiesare susceptible to oxidation, particularly in the presence of transitionmetal ions, thereby forming an o-quinone, which ultimately undergoes acrosslinking reaction with another catechol-type moiety. The presumedcrosslinking reaction is shown in Scheme 1 below.

Although these types of adhesive proteins and others can be easilysynthesized by biological organisms, such proteins represent a muchgreater challenge for commercial production and field applications interms of synthetic difficulty and cost. Furthermore, protein-derivedbiomaterials may provide poor stability at elevated temperatures and/orin certain types of chemical environments.

Given the beneficial properties of bioadhesives, it would be desirableto apply similar adhesives in a non-biological setting, particularly inenvironments where traditional adhesives may be less adherent or haveinsufficient strength, such as in aqueous environments. As noted above,in non-biological settings, protein molecules can present considerablesynthetic and economic challenges that may prohibit their successfulimplementation. DOPA-containing proteins may be particularly challengingin this regard. Not only is DOPA very expensive, but chemicalinstability of its catechol moiety can make synthetic manipulationsdifficult.

Subterranean treatment operations are one field application where it cansometimes be desirable to utilize adhesive compositions. Adhesivecompositions can be used in subterranean formations, for example, toconsolidate a loosely consolidated formation, to improve structuralintegrity of the wellbore, to consolidate a particulate pack (e.g., aproppant pack or a gravel pack) in the subterranean formation, tocontrol the production of fines, and the like. Aqueous tackifyingagents, non-aqueous tackifying agents, curable resin tackifying agents,and non-curable and non-aqueous tackifying agents can be used in thisregard in subterranean treatment operations. Although these tackifyingagents and others can often be successfully used in subterraneantreatment operations, there may still be certain applications in whichthey are chemically unstable or are otherwise difficult to deployoperationally. Furthermore, some components of traditional adhesivecompositions can present challenges from the standpoint ofbiodegradability or environmentally acceptability.

SUMMARY OF THE INVENTION

The present disclosure relates to adhesive compositions, and, morespecifically, to biomimetic adhesive compositions and their use in asubterranean formation.

In some embodiments, the present invention provides a method comprising:providing an adhesive composition comprising: a first polymer comprisinga plurality of monomers that comprise a phenolic moiety; a biopolymerthat is crosslinkable with the first polymer; a crosslinking agent; andan oxidizing agent; introducing the adhesive composition into asubterranean formation; and forming a coacervate-bound surface in thesubterranean formation by crosslinking the first polymer.

In some embodiments, the present invention provides a method comprising:providing an adhesive composition comprising: a first polymer comprisinga plurality of monomers that comprise a 1,2-dihydroxybenzene moiety; asecond polymer that is crosslinkable with the first polymer; an optionalcrosslinking agent; and an oxidizing agent; introducing the adhesivecomposition into a subterranean formation; oxidizing at least a portionof the 1,2-dihydroxybenzene moieties so as to crosslink the firstpolymer; and forming a coacervate-bound surface in the subterraneanformation from the adhesive composition.

In some embodiments, the present invention provides an adhesivecomposition comprising: a first polymer comprising a plurality ofmonomers that comprise a 1,2-dihydroxybenzene moiety; a second polymerthat is crosslinkable with the first polymer; an optional crosslinkingagent; and an oxidizing agent.

The features and advantages of the present invention will be readilyapparent to one having ordinary skill in the art upon a reading of thedescription of the preferred embodiments that follows.

DETAILED DESCRIPTION

The present disclosure relates to adhesive compositions, and, morespecifically, to biomimetic adhesive compositions and their use in asubterranean formation.

In the context of the present disclosure, we have discovered adhesivecompositions that are biomimetic in nature and have been inspired by thebioadhesives produced by marine mussels. Marine mussel bioadhesives arepolyphenolic proteins that are believed to be non-toxic andenvironmentally benign. Although the adhesion of marine mussels andother marine organisms to surfaces can be a nuisance in some cases(e.g., barnacle adhesion to ships), the strength and utility of thebioadhesive itself is not in doubt. Given the beneficial properties ofbioadhesives, it would be desirable to apply like adhesive compositionsin a non-biological setting, particularly in environments wheretraditional adhesives may be less adherent or have insufficientstrength, such as in aqueous environments, including those encounteredduring subterranean treatment operations.

In view of the previously described difficulties associated withproteins, particularly DOPA-containing proteins, we have designedadhesive compositions that are biomimetic in nature and incorporate themore desirable functional aspects of marine mussel bioadhesives whileaddressing potential cost, stability, and synthetic concerns. Theadhesive compositions described herein may be particularly desirable foruse in aqueous environments, including those commonly encountered duringsubterranean treatment operations.

The adhesive compositions described herein may be advantageous overthose presently in use for subterranean treatment operations due totheir biological inspiration. Because the adhesive compositions arebiologically inspired, they may have a smaller environmental footprintthan do other synthetic adhesive compositions that are currently used insubterranean treatment operations. Likewise, the adhesive compositionsmay be particularly well suited for use in an aqueous environment.

Even if the parent bioadhesives could be successfully utilized in anon-biological setting, it is believed that the adhesive compositionsdescribed herein may present certain additional advantages over theparent bioadhesive itself, particularly when used in a non-biologicalsetting. First, the adhesive compositions described herein can comprisean adhesive substance that is structurally related to but modified fromthe adhesive protein of the parent bioadhesive. The adhesive substancemay retain the adhesion properties of the parent bioadhesive whileimproving its stability and lowering its synthesis costs. Thesemodifications are described in more detail hereinafter. Second, theadhesive compositions described herein can comprise a diluent polymerthat does not contain catechol-type moieties and is crosslinkable withthe adhesive substance. Inclusion of the diluent polymer may furtherlower costs of the adhesive compositions by allowing smaller quantitiesof the adhesive substance to be used while still achieving goodadhesion. Inclusion of the diluent polymer may provide the bulk neededfor the adhesive compositions to form a coacervate-bound surface, and/orthe diluent polymer may guide the self-assembly formation of thecoacervate-bound surface in some cases. In this regard, the diluentpolymer itself may have good mechanical strength but not be capable ofstrongly binding to a surface alone. However, the adhesive substance andthe diluent polymer may work in concert in the present adhesivecompositions, with the adhesive substance providing surface adherenceand the diluent polymer providing bulk and enhancing mechanicalstrength, particularly when the adhesive substance and the diluentpolymer are crosslinked with one another. In addition, the diluentpolymer may be chosen to further tune the properties of the adhesivecompositions. For example, the diluent polymer may be chosen to have aspecified mechanical strength or to be degradable, such that theadhesive composition eventually degrades. In some embodiments, thediluent polymer may comprise a biopolymer, which can further support theenvironmental favorability of the adhesive compositions describedherein.

As noted above, the adhesive compositions described herein can comprisean adhesive substance that is structurally related to but modified fromthe adhesive protein of the parent bioadhesive. These modifications mayimprove stability, lessen synthetic difficulties, and reduce costsassociated with the adhesive compositions described herein. In someembodiments of the present invention, we have replaced the peptidicbackbone of the adhesive protein, at least in part, with a non-peptidicpolymer backbone. This replacement can improve stability and lessen thechallenges associated with polypeptide synthesis, particularlylarge-scale polypeptide synthesis. Furthermore, in some or otherembodiments of the present invention, we have replaced DOPA with othercatechol-type moieties, which may further improve stability and lowercosts. In addition, the amount of catechol-type moieties included in theadhesive substance may be adjusted to promote a desired degree ofadhesion. By keeping the amount of catechol-type moieties to the minimumamount necessary to achieve a desired degree of adhesion, chemicalstability may be improved and costs may be lowered. In still otherembodiments of the present invention, at least some of the catechol-typemoieties may be replaced with simple phenolic moieties (e.g.,non-catechol monophenols) to achieve an adhesive composition having likeadhesive properties.

In various embodiments of the present invention, the adhesivecompositions described herein may be introduced into a subterraneanformation in order to treat the subterranean formation. When used totreat a subterranean formation, the adhesive compositions may beintroduced into the subterranean formation in a treatment fluid. As usedherein, the term “treatment fluid” refers to a fluid that is placed in asubterranean formation in order to perform a desired function. Treatmentfluids can be used in a variety of subterranean treatment operations,including, but not limited to, drilling operations, productiontreatments, stimulation treatments, remedial treatments, fluid diversionoperations, fracturing operations, secondary or tertiary enhanced oilrecovery (EOR) operations, and the like. As used herein, the terms“treat,” “treatment,” “treating,” and other grammatical equivalentsthereof refer to any subterranean operation that uses a fluid inconjunction with performing a desired function and/or achieving adesired purpose. The terms “treat,” “treatment,” and “treating,” as usedherein, do not imply any particular action by the fluid or anyparticular component thereof unless otherwise specified. Treatmentfluids can include, for example, drilling fluids, fracturing fluids,acidizing fluids, conformance treatment fluids, damage control fluids,remediation fluids, scale removal and inhibition fluids, chemicalfloods, and the like. In some embodiments of the present invention,treatment fluids containing the adhesive compositions described hereinmay be used in a subterranean formation for operations such as, forexample, wellbore consolidation, particulate pack consolidation (e.g.,proppant pack consolidation or gravel pack consolidation), finescontrol, and the like. In some embodiments of the present invention, theadhesive compositions may form a coacervate-bound surface in thesubterranean formation.

In some embodiments of the present invention, the treatment fluids maycomprise an aqueous carrier fluid as their continuous phase. Suitableaqueous carrier fluids may include, for example, fresh water, acidifiedwater, salt water, seawater, brine (e.g., a saturated salt solution), oran aqueous salt solution (e.g., a non-saturated salt solution). Theaqueous carrier fluids can be obtained from any suitable source. Inother embodiments of the present invention, the treatment fluids maycomprise an organic solvent, such as hydrocarbons, as their continuousphase.

In some embodiments of the present invention, adhesive compositionsdescribed herein may comprise: a first polymer comprising a plurality ofmonomers that comprise a phenolic moiety; a second polymer that iscrosslinkable with the first polymer; a crosslinking agent; and anoxidizing agent. In some embodiments, at least some of the phenolicmoieties may comprise a 1,2-dihydroxybenzene moiety. In someembodiments, the second polymer may comprise a biopolymer.

In some embodiments of the present invention, adhesive compositionsdescribed herein may comprise: a first polymer comprising a plurality ofmonomers that comprise a phenolic moiety; a biopolymer that iscrosslinkable with the first polymer; a crosslinking agent; and anoxidizing agent.

In some embodiments of the present invention, adhesive compositionsdescribed herein may comprise: a first polymer comprising a plurality ofmonomers that comprise a 1,2-dihydroxybenzene moiety; a second polymerthat is crosslinkable with the first polymer; an optional crosslinkingagent; and an oxidizing agent.

In some embodiments of the present invention, adhesive compositionsdescribed herein may comprise: a first polymer comprising a plurality ofmonomers that comprise a 1,2-dihydroxybenzene moiety; a biopolymer thatis crosslinkable with the first polymer; an optional crosslinking agent;and an oxidizing agent.

As used herein, the term “1,2-dihydroxybenzene” is used interchangeablywith the term “catechol.” As used herein, the terms“1,2-dihydroxybenzene” and “catechol” refer to an aromatic ring that hasphenolic hydroxy groups present on adjacent ring carbon atoms. Referenceto 1,2-substitution simply refers to the disposition of the phenolichydroxy groups relative to one another, not to the conventional IUPACnumbering system or any related numbering system of the substituents onthe aromatic ring.

Without being bound by any theory or mechanism, it is believed thatphenolic polymers comprising a 1,2-dihydroxybenzene moiety (e.g., acatechol-type moiety) may crosslink at a greater rate and to a greaterextent than do non-catechol phenolic polymers. Remaining unbound bytheory or mechanism, it is believed that the source of this effect isnot just the greater quantity of phenolic hydroxyl groups present incatechol-containing phenolic polymers. Rather, it is believed that theability of catechols to form o-quinones may promote crosslinking,potentially in a manner similar to that shown in Scheme 1 above. Itshould be recognized, however, that crosslinking need not necessarilytake place as depicted in Scheme 1. For example, in some embodiments ofthe present invention, an optional crosslinking agent may promoteinternal crosslinking within the first polymer and/or externally betweenthe first polymer and the second polymer. In other embodiments of thepresent invention, crosslinking may take place directly without theoptional crosslinking agent being present. Unless otherwise specifiedherein, any statement regarding crosslinking should not be construed toimply any particular mechanism of crosslinking or type of crosslinkformed. In the embodiments described herein, it is to be recognized thatthe first polymer comprising phenolic moieties may be internallycrosslinked to itself, externally crosslinked with the second polymer,or both. In some embodiments of the present invention, a crosslinkingagent may form the crosslinks. In other embodiments of the presentinvention, crosslinking may be direct, similar to the crosslinkingdepicted in Scheme 1. That is, in such embodiments, the crosslinkingagent may be absent. As described above, crosslinking of the firstpolymer to the second polymer may be particularly advantageous fortuning the properties of the adhesive compositions described herein.

In some embodiments of the present invention, the first polymer maycomprise a homopolymer. That is, in such embodiments, the first polymermay comprise a homopolymer of monomers that comprise a phenolic moiety.In some embodiments of the present invention, the first polymer maycomprise a homopolymer of monomers that comprise a 1,2-dihydroxybenzenemoiety.

In some embodiments of the present invention, the first polymer maycomprise a copolymer of the monomers comprising the phenolic moiety.That is, in such embodiments, the first polymer may comprise at leasttwo different types of monomer units. Such copolymers may be block,random, graft, or any combination thereof, for example. In someembodiments of the present invention, the copolymer comprising the firstpolymer may comprise a mixture of monomers where some of the monomerscomprise a simple phenolic moiety (e.g., a non-catechol moiety) and someof the monomers comprise a 1,2-dihydroxybenzene moiety (e.g., acatechol-type moiety). In some embodiments of the present invention,additional monomers not comprising a phenolic moiety may further bepresent.

In some embodiments of the present invention, the first polymer maycomprise a copolymer of monomers comprising the phenolic moiety and atleast one other copolymer unit. In some embodiments of the presentinvention, the first polymer may comprise a copolymer of monomerscomprising a 1,2-dihydroxybenzene moiety and at least one othercopolymer unit. In some embodiments of the present invention, the atleast one other copolymer unit may lack a phenolic moiety. That is, acopolymer unit lacking a phenolic moiety may be copolymerized withmonomers comprising a phenolic moiety and/or monomers comprising a1,2-dihydroxybenzene moiety. Suitable copolymer units that may becopolymerized with monomers comprising a phenolic moiety and/or monomerscomprising a 1,2-dihydroxybenzene moiety may include, for example,styrenic polymer units, vinylic polymer units (e.g., polyalkylenepolymer units), polyether polymer units (e.g., polyethylene glycolpolymer units), fluoropolymer units, and any combination thereof. Insome embodiments, monomers such as, for example, hydroxyproline,dihydroxyproline, 4-hydroxyarginine, O-phosphoserine, any derivativethereof, and any combination thereof may be copolymerized with monomerscomprising a phenolic moiety and/or monomers comprising a1,2-dihydroxybenzene moiety.

In some embodiments of the present invention, the first polymercomprising the phenolic moiety and/or the 1,2-dihydroxybenzene moietymay not comprise a peptidic polymer backbone. That is, in suchembodiments, the first polymer may comprise a non-peptidic polymer. Asused herein, the term “non-peptidic polymer” refers to a polymer thatdoes not comprise amino acid oligomers within its polymer backbone. Asused herein, the term “amino acid oligomer” refers to 5 or morecontiguous amino acids joined in series by peptidic bonds. As usedherein, the term “peptidic bond” refers to an amide bond formed betweenthe α-amino group of a first amino acid and the carboxylic acid group ofa second amino acid. That is, in some embodiments of the presentinvention, a non-peptidic polymer may entirely lack peptidic bonds oronly have 5 or less contiguous amino acids within its polymer backbone.However, it should be noted that a “non-peptidic polymer” may stillcomprise a polyamide, where at least some of the amide bonds of thepolymer backbone are not peptidic bonds. In such embodiments of thepresent invention, “non-peptidic polymers” may still comprise at leastsome amino acid monomers within their polymer backbones. In someembodiments of the present invention, suitable non-peptidic polymers foruse in the adhesive compositions described herein may comprise polymerbackbones such as, for example, polyamides, polyalkylenes (includingpolystyrenes), polyesters, polyoxyalkylenes, polyurethanes, and thelike, including copolymers thereof, where the phenolic moieties arepresent as the polymer side chains.

In some embodiments of the present invention, the first polymer maycomprise a plurality of side chains that comprise a simple phenol (e.g.,a non-catechol moiety). In some embodiments of the present invention,the first polymer may comprise a plurality of side chains that comprisea 1,2-dihydroxybenzene moiety (e.g., a catechol-type moiety). In someembodiments of the present invention, the first polymer may comprise aplurality of side chains, where some of the side chains comprise asimple phenol and some of the side chains comprise a1,2-dihydroxybenzene moiety.

In some embodiments of the present invention, monomers that comprise aphenolic moiety may have the following structure (Structure 1):

where P₁ represents a polymerizable group and Q₁ represents any type offunctionality on the aromatic ring. Any number of Q₁ from 0 to 4 may bepresent on the aromatic ring in any substitution pattern. Furthermore,P₁ may be present in any configuration relative to the hydroxyl groupand any Q₁ substitution present.

In some embodiments of the present invention, monomers that comprise a1,2-dihydroxybenzene moiety may have the following structure:

where P₁ represents a polymerizable group and Q₁ represents any type offunctionality on the aromatic ring. Any number of Q₁ from 0 to 3 may bepresent on the aromatic ring in any substitution pattern. Furthermore,P₁ may be present in any configuration relative to the hydroxyl groupsand any Q₁ substitution present. In some embodiments of the presentinvention, monomers that comprise a 1,2-dihydroxybenzene moiety maycomprise polymerizable derivatives of 1,2-dihydroxybenzene compounds or1,2,3-trihydroxybenzene compounds. Suitable monomers that comprise a1,2-dihydroxybenzene moiety may include polymerizable derivatives of1,2-dihydroxybenzene or 1,2,3-trihydroxybenzene compounds such as, forexample, catechol, pyrogallol, 1,2,4-benzenetriol,2,4,5-trihydroxybenzoic acid, 3,4,5-trihydroxybenzoic acid (gallicacid), 2,3,4-trihydroxybenzoic acid, 2,3-dihydroxybenzoic acid,3,4-dihydroxybenzoic acid, 6,7-dihydroxycoumarin, ellagic acid,urushiols, chlorogenic acid, caffeic acid, and like compounds. It isbelieved that 1,2,3-trihydroxybenzene compounds may function similarlyto 1,2-dihydroxybenzene compounds in the present embodiments in theirability to form an o-quinone. In some embodiments of the presentinvention, suitable 1,2-dihydroxybenzene compounds may include3,4-dihydroxyphenylalanine (DOPA), dopamine, any polymerizablederivative thereof, or any combination thereof.

The amount of phenolic moieties or 1,2-dihydroxybenzene moieties toinclude in the first polymer may vary over a wide range. When only thephenolic moieties or the 1,2-dihydroxybenzene moieties are present(e.g., in a homopolymer), the first polymer may comprise 100% phenolicmoieties or 1,2-dihydroxybenzene moieties by weight, expressed as weightpercent of the monomer comprising the phenolic moiety or the1,2-dihydroxybenzene moiety. In copolymer embodiments, an amount of thephenolic moieties or 1,2-dihydroxybenzene moieties may range betweenabout 5% and about 80% by weight of the first polymer, expressed asweight percent of the monomer comprising the phenolic moiety or the1,2-dihydroxybenzene moiety. In some copolymer embodiments, an amount ofthe phenolic moieties or 1,2-dihydroxybenzene moieties may range betweenabout 10% and about 40% by weight of the first polymer, expressed asweight percent of the monomer comprising the phenolic moiety or the1,2-dihydroxybenzene moiety.

As described above, a second polymer may be included in the adhesivecompositions described herein, and there may be a number of advantagesto be realized in doing so. For example, it may be desirable to utilizequantities of the first polymer that are as small as possible in orderto keep production costs low while still achieving a satisfactory degreeof adhesion. In some embodiments of the present invention, the secondpolymer may comprise at least about 50% of the adhesive composition. Insome embodiments of the present invention, a ratio of the first polymerto the second polymer can range between about 1:1 to about 1:10. In someembodiments of the present invention, a ratio of the first polymer tothe second polymer can range between about 1:1 to about 1:5.

In various embodiments of the present invention, the second polymer maybe crosslinkable with the first polymer, where crosslinking may takeplace in any manner, optionally in the presence of a crosslinking agent.Although the second polymer may be crosslinkable with the first polymer,it is not necessarily required to do so. For example, in someembodiments of the present invention, crosslinking that does take placein the present adhesive compositions may occur internally within thefirst polymer, with the second polymer remaining unbound to the firstpolymer. However, in some embodiments of the present invention, thefirst polymer may be crosslinked to the second polymer, particularlyafter exposure to a crosslinking agent under conditions suitable topromote crosslinking. In some embodiments of the present invention, bothtypes of crosslinking may be present. It is again to be emphasized thatthe crosslinking agent may be optional. In particular, when the firstpolymer comprises a 1,2-dihydroxybenzene moiety and the second polymercomprises an amine, a crosslinking agent may not be necessary to affectcrosslinking between the first polymer and the second polymer.

In some embodiments of the present invention, crosslinking of the firstpolymer may take place after its oxidation. For example, oxidation of afirst polymer comprising a 1,2-dihydroxybenzene moiety may promotecrosslinking with the second polymer (e.g., through formation of ano-quinone). In other embodiments of the present invention, the firstpolymer may be crosslinked without oxidation taking place. For example,in some embodiments, when the first polymer comprises a simple phenolicmoiety, crosslinking of the first polymer to the second polymer may takeplace without oxidation of the first polymer occurring. That is, in suchembodiments, the unoxidized phenolic moieties may be crosslinkeddirectly through a reaction with a crosslinking agent. In alternativeembodiments, a simple phenolic moiety may be crosslinked afteroxidation. In embodiments in which the first polymer comprises aplurality of monomers comprising a 1,2-dihydroxybenzene moiety, the1,2-dihydroxybenzene moieties may be completely oxidized to an o-quinonein some embodiments, or a mixture of unoxidized and oxidized1,2-dihydroxybenzene moieties may be present in other embodiments.

In some embodiments of the present invention, particularly suitableexamples of the second polymer may comprise a plurality of chargedmoieties. In some embodiments of the present invention, the chargedmoieties may bear a positive charge. In other embodiments of the presentinvention, the charged moieties may bear a negative charge. It isbelieved that use of a charged second polymer may promote the formationof a coacervate when the adhesive compositions are allowed to cure.Without being bound by any theory or mechanism, it is believed that asecond polymer comprising a plurality of charged moieties may decreasethe energy barrier of a mineral surface being bonded by the coacervate,thereby promoting more effective interaction and stronger bondingtherewith. For example, mineral surfaces, including those found in asubterranean formation, may be in a water-wet state with a thin filmbarrier of water over underlying surface hydroxyl groups. It is believedthat a charged second polymer may increase compatibility with thiswater-wet state.

In some embodiments of the present invention, the second polymer maycomprise a biopolymer. In some embodiments of the present invention, thebiopolymer may be charged or capable of bearing a charge, depending onpH conditions. Suitable biopolymers may include, for example, chitosan,collagen, keratin, elastin, chitin, cellulose, mucin, any derivativethereof, and any combination thereof. Particularly suitable derivativesmay include carboxylic acid- or amine-containing biopolymers orderivatives thereof that can bear a negative charge or a positivecharge, respectively. In some embodiments of the present invention, aparticularly suitable biopolymer may comprise chitosan or a derivativethereof. In embodiments in which chitosan is used, crosslinking betweenthe chitosan molecules and the first polymer may take place through theamino group of the chitosan molecules.

In some embodiments of the present invention, a crosslinking agent maybe used to promote crosslinking of the first polymer. However, in otherembodiments of the present invention, crosslinking of the first polymermay occur without the crosslinking agent being present. For example, insome embodiments of the present invention, a first polymer comprising aplurality of monomers comprising a 1,2-dihydroxybenzene moiety may becrosslinked after oxidation without a crosslinking agent being present.In some embodiments of the present invention, suitable crosslinkingagents may include transition metal ions. In other embodiments of thepresent invention, organic crosslinking agents may be used. In someembodiments of the present invention, suitable organic crosslinkingagents may include amine-containing compounds, amine-containingoligomers, or amine-containing polymers such as, for example,polyalkyleneimines and polyalkylenepolyamines. In some embodiments ofthe present invention, a suitable crosslinking agent may comprisepolyethyleneimine. In some embodiments of the present invention, atransition metal ion crosslinking agent may play a dual role incrosslinking and oxidizing the first polymer. In some embodiments of thepresent invention, the transition metal ion may be encountered when thecompositions are used in forming a coacervate-bound surface. Forexample, in some embodiments of the present invention, the adhesivecompositions may encounter a transition metal ion or other metal ionthat promotes crosslinking when used in conjunction with a subterraneantreatment operation. That is, in some embodiments of the presentinvention, the adhesive compositions may be crosslinked by a metal ionencountered within a subterranean formation.

In some embodiments of the present invention, suitable oxidizing agentsmay include, for example, a transition metal ion, an oxidizing anion, aperoxide, or any combination thereof. In some embodiments of the presentinvention, suitable oxidizing anions may include, for example,perborate, percarbonate, chlorate, chlorite, bromate, periodate, or anycombination thereof. In some embodiments, the oxidizing agent maycomprise a transition metal ion that also serves as a crosslinkingagent.

In some embodiments of the present invention, the adhesive compositionsdescribed herein may further comprise an additional polymer that isnon-crosslinkable with the first polymer. Inclusion of such anadditional polymer may be used to further modify the properties of theadhesive compositions. In general, any type of polymer, includingbiopolymers, may be used as the additional polymer, as long as theadditional polymer does not form crosslinks with the first polymer and,optionally, the second polymer.

In some embodiments of the present invention, the adhesive compositionsdescribed herein may be used in subterranean treatment operations.Although any subterranean treatment operation lies within the scope ofthe present embodiments, particularly suitable subterranean operationsmay include wellbore and near-wellbore consolidation operations,particulate pack consolidation, fracture stabilization, and finescontrol, for example.

In some embodiments of the present invention, the adhesive compositionsdescribed herein may be used in a fracturing operation. For example, theadhesive compositions described herein may be formulated in a fracturingfluid that is used to fracture the subterranean formation. Thereafter,the adhesive compositions may undergo crosslinking so as to form acoacervate-bound surface in the subterranean formation. When used in afracturing operation, the fracturing fluid may be introduced to thesubterranean formation at a pressure sufficient to create or extend atleast one fracture in the subterranean formation.

In some embodiments of the present invention, methods described hereinmay comprise: providing an adhesive composition that comprises a firstpolymer comprising a plurality of monomers that comprise a phenolicmoiety, a biopolymer that is crosslinkable with the first polymer, acrosslinking agent, and an oxidizing agent; introducing the adhesivecomposition into a subterranean formation; and forming acoacervate-bound surface in the subterranean formation by crosslinkingthe first polymer.

In some embodiments of the present invention, methods described hereinmay comprise: providing an adhesive composition that comprises a firstpolymer comprising a plurality of monomers that comprise a1,2-dihydroxybenzene moiety, a second polymer that is crosslinkable withthe first polymer, an optional crosslinking agent, and an oxidizingagent; introducing the adhesive composition into a subterraneanformation; oxidizing at least a portion of the 1,2-dihydroxybenzenemoieties so as to crosslink the first polymer; and forming acoacervate-bound surface in the subterranean formation. In someembodiments of the present invention, the second polymer may comprise abiopolymer.

In some embodiments of the present invention, forming a coacervate-boundsurface in the subterranean formation may comprise consolidating awellbore surface or consolidating a plurality of particulates in thesubterranean formation. Consolidating a wellbore surface may stabilizethe wellbore surface in loosely consolidated formations. In someembodiments of the present invention, consolidating a plurality ofparticulates may comprise consolidating a proppant pack. In otherembodiments of the present invention, consolidating a plurality ofparticulates may comprise consolidating a gravel pack. Consolidation ofa particulate pack may reduce the amount of particulates produced fromthe subterranean formation. In still other embodiments of the presentinvention, consolidating a plurality of particulates may comprisecontrolling fines in the subterranean formation. In some embodiments,formation of a coacervate-bound surface in the subterranean formationmay occur subsequent to a fracturing operation.

In some embodiments of the present invention, the first polymer may becrosslinked to the second polymer or to the biopolymer. In someembodiments of the present invention, the first polymer may beinternally crosslinked with itself. In still other embodiments of thepresent invention, the first polymer may be both internally crosslinkedand crosslinked to the second polymer or to the biopolymer.

Therefore, the present invention is well adapted to attain the ends andadvantages mentioned as well as those that are inherent therein. Theparticular embodiments disclosed above are illustrative only, as thepresent invention may be modified and practiced in different butequivalent manners apparent to those skilled in the art having thebenefit of the teachings herein. Furthermore, no limitations areintended to the details of construction or design herein shown, otherthan as described in the claims below. It is therefore evident that theparticular illustrative embodiments disclosed above may be altered,combined, or modified and all such variations are considered within thescope and spirit of the present invention. The invention illustrativelydisclosed herein suitably may be practiced in the absence of any elementthat is not specifically disclosed herein and/or any optional elementdisclosed herein. While compositions and methods are described in termsof “comprising,” “containing,” or “including” various components orsteps, the compositions and methods can also “consist essentially of” or“consist of” the various components and steps. All numbers and rangesdisclosed above may vary by some amount. Whenever a numerical range witha lower limit and an upper limit is disclosed, any number and anyincluded range falling within the range is specifically disclosed. Inparticular, every range of values (of the form, “from about a to aboutb,” or, equivalently, “from approximately a to b,” or, equivalently,“from approximately a-b”) disclosed herein is to be understood to setforth every number and range encompassed within the broader range ofvalues. Also, the terms in the claims have their plain, ordinary meaningunless otherwise explicitly and clearly defined by the patentee.Moreover, the indefinite articles “a” or “an,” as used in the claims,are defined herein to mean one or more than one of the element that itintroduces. If there is any conflict in the usages of a word or term inthis specification and one or more patent or other documents that may beincorporated herein by reference, the definitions that are consistentwith this specification should be adopted.

The invention claimed is:
 1. An adhesive composition comprising: a firstpolymer comprising a plurality of monomers that comprise a1,2-dihydroxybenzene moiety; a second polymer that is crosslinkable withthe first polymer; and an oxidizing agent.
 2. The adhesive compositionof claim 1, wherein the first polymer is internally crosslinked,crosslinked with the second polymer, or both.
 3. The adhesivecomposition of claim 2, further comprising: a crosslinking agent.
 4. Theadhesive composition of claim 3, wherein the crosslinking agentcomprises a transition metal ion.
 5. The adhesive composition of claim1, wherein the second polymer comprises a biopolymer selected from thegroup consisting of chitosan, collagen, keratin, elastin, chitin,cellulose, mucin, any derivative thereof, and any combination thereof.6. The adhesive composition of claim 1, wherein the first polymercomprises a copolymer of the monomers comprising the1,2-dihydroxybenzene moiety and at least one other copolymer unit. 7.The adhesive composition of claim 6, wherein the at least one othercopolymer unit comprises a styrenic polymer unit, a vinylic polymerunit, a polyether polymer unit, a fluoropolymer unit, or a polymer unitcomprising a monomer selected from the group consisting ofhydroxyproline, dihydroxyproline, 4-hydroxyarginine, O-phosphoserine,any derivative thereof, and any combination thereof.
 8. The adhesivecomposition of claim 1, wherein the oxidizing agent comprises atransition metal ion; an oxidizing anion selected from the groupconsisting of perborate, percarbonate, chlorate, chlorite, bromate,periodate, and any combination thereof; a peroxide; or any combinationthereof.
 9. The adhesive composition of claim 1, further comprising: anon-crosslinkable polymer.
 10. An adhesive composition comprising: afirst polymer comprising a plurality of monomers that comprise a1,2-dihydroxybenzene moiety; a second polymer that is crosslinkable withthe first polymer; a crosslinking agent; non-crosslinkable polymer; and,an oxidizing agent.
 11. The adhesive composition of claim 10, whereinthe first polymer is internally crosslinked, crosslinked with the secondpolymer, or both.
 12. The adhesive composition of claim 10, wherein thecrosslinking agent comprises a transition metal ion.
 13. The adhesivecomposition of claim 10, wherein the second polymer comprises abiopolymer selected from the group consisting of chitosan, collagen,keratin, elastin, chitin, cellulose, mucin, any derivative thereof, andany combination thereof.
 14. The adhesive composition of claim 10,wherein the first polymer comprises a copolymer of the monomerscomprising the 1,2-dihydroxybenzene moiety and at least one othercopolymer unit.
 15. The adhesive composition of claim 10, wherein thefirst polymer comprises a copolymer of the monomers comprising the1,2-dihydroxybenzene moiety and at least one other copolymer unit. 16.The adhesive composition of claim 15, wherein the at least one othercopolymer unit comprises a styrenic polymer unit, a vinylic polymerunit, a polyether polymer unit, a fluoropolymer unit, or a polymer unitcomprising a monomer selected from the group consisting ofhydroxyproline, dihydroxyproline, 4-hydroxyarginine, O-phosphoserine,any derivative thereof, and any combination thereof.
 17. The adhesivecomposition of claim 10, wherein the oxidizing agent comprises atransition metal ion; an oxidizing anion selected from the groupconsisting of perborate, percarbonate, chlorate, chlorite, bromate,periodate, and any combination thereof; a peroxide; or any combinationthereof.